EP1272240B1 - Seringue hypodermique - Google Patents

Seringue hypodermique Download PDF

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Publication number
EP1272240B1
EP1272240B1 EP01911998.1A EP01911998A EP1272240B1 EP 1272240 B1 EP1272240 B1 EP 1272240B1 EP 01911998 A EP01911998 A EP 01911998A EP 1272240 B1 EP1272240 B1 EP 1272240B1
Authority
EP
European Patent Office
Prior art keywords
needle
syringe
housing
plunger
sheath
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP01911998.1A
Other languages
German (de)
English (en)
Other versions
EP1272240B8 (fr
EP1272240A1 (fr
Inventor
David William Parker
Colin Hamilton Burgess
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
C Major Ltd
Original Assignee
C Major Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by C Major Ltd filed Critical C Major Ltd
Publication of EP1272240A1 publication Critical patent/EP1272240A1/fr
Application granted granted Critical
Publication of EP1272240B1 publication Critical patent/EP1272240B1/fr
Publication of EP1272240B8 publication Critical patent/EP1272240B8/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
    • A61M5/321—Means for protection against accidental injuries by used needles
    • A61M5/3243—Means for protection against accidental injuries by used needles being axially-extensible, e.g. protective sleeves coaxially slidable on the syringe barrel
    • A61M5/326—Fully automatic sleeve extension, i.e. in which triggering of the sleeve does not require a deliberate action by the user
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M2005/3103—Leak prevention means for distal end of syringes, i.e. syringe end for mounting a needle
    • A61M2005/3107—Leak prevention means for distal end of syringes, i.e. syringe end for mounting a needle for needles
    • A61M2005/3109—Caps sealing the needle bore by use of, e.g. air-hardening adhesive, elastomer or epoxy resin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
    • A61M5/321—Means for protection against accidental injuries by used needles
    • A61M5/322—Retractable needles, i.e. disconnected from and withdrawn into the syringe barrel by the piston
    • A61M5/3234—Fully automatic needle retraction, i.e. in which triggering of the needle does not require a deliberate action by the user
    • A61M2005/3241—Needle retraction energy is accumulated inside of a hollow plunger rod
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
    • A61M5/321—Means for protection against accidental injuries by used needles
    • A61M5/322—Retractable needles, i.e. disconnected from and withdrawn into the syringe barrel by the piston
    • A61M5/3234—Fully automatic needle retraction, i.e. in which triggering of the needle does not require a deliberate action by the user
    • A61M2005/3241—Needle retraction energy is accumulated inside of a hollow plunger rod
    • A61M2005/3242—Needle retraction by vacuum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
    • A61M5/321—Means for protection against accidental injuries by used needles
    • A61M5/3243—Means for protection against accidental injuries by used needles being axially-extensible, e.g. protective sleeves coaxially slidable on the syringe barrel
    • A61M5/326—Fully automatic sleeve extension, i.e. in which triggering of the sleeve does not require a deliberate action by the user
    • A61M2005/3261—Fully automatic sleeve extension, i.e. in which triggering of the sleeve does not require a deliberate action by the user triggered by radial deflection of the anchoring parts between sleeve and syringe barrel, e.g. spreading of sleeve retaining hooks having slanted surfaces by engagement with conically shaped collet of the piston rod during the last portion of the injection stroke of the plunger
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3202—Devices for protection of the needle before use, e.g. caps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/50—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile
    • A61M5/5013—Means for blocking the piston or the fluid passageway to prevent illegal refilling of a syringe
    • A61M5/502—Means for blocking the piston or the fluid passageway to prevent illegal refilling of a syringe for blocking the piston

Definitions

  • This invention relates to hypodermic syringes with a retractable needle.
  • hypodermic syringes with retractable needles have been proposed.
  • a hypodermic syringe including a housing, a plunger, a needle carrier with a needle mounted thereto positionable within the housing with the needle extending therefrom, a sheath mounted to the needle carrier and surrounding the needle, and a spring, the plunger and the spring configured in such a way that when the syringe is used and the plunger reaches the needle carrier it becomes attached thereto and stored energy in the spring is released to retract the needle carrier into the housing.
  • FR 2739564 describes a syringe with a barrel for containing injectant and receiving plunger.
  • a needle assembly is retractable into a retraction tube adjacent to the barrel.
  • the barrel is in fluid communication with the needle via a lateral channel.
  • a syringe including a needle retractable by stored energy on completion of an injection stroke, comprising a housing and a plunger, characterised in that a sealed capsule assembly containing the injectant is mounted in the housing and the sealed capsule assembly includes a needle assembly comprising a needle mounting, a needle, a frangible seal and a needle sheath covering the needle, wherein the sealed needle sheath prevents movement of the plunger into the housing before the seal is broken and the sheath is removed.
  • a syringe which may be pre-charged with injectant, and for which the needle is automatically withdrawn after use to avoid the risk of needle stick injury.
  • Figure 1 illustrates an embodiment of syringe in accordance with the invention which comprise a capsule assembly 1 which is pre-charged with injectant and includes the needle assembly with a needle sheath as will be described in more detail hereinafter.
  • the capsule assembly is mounted in a cylindrical barrel 2 in which is mounted a plunger 3 provided with a closure piece 4 and a piston 5.
  • the capsule 1 containing injectant is integral with a needle mounting 1.1 and a needle 1.2.
  • the needle mounting 1.1 contains a frangible sealant 1.3 to give a positive retention for a needle sheath 1.4.
  • the capsule assembly is of a diameter to fit through an opening 2.1 in the barrel 2 that has a region 1.5 of increased diameter in order to locate the capsule in place.
  • the open end of the capsule 1 has an internal lip 1.6 and an external lip 1.7 and is provided with a resilient plunger disc 1.8.
  • the needle end of the capsule 1.9 is dished.
  • Injectant 1.10 is pre-charged into the capsule assembly 1 between the disc 1.8 and the dished end 1.9.
  • the barrel 2 has a nose 2.1, the aperture of which is larger than the diameter of the needle sheath 1.4.
  • One or more arms 2.2 which may be part of the barrel 2, are positioned so that they abut against the external lip 1.7 of the capsule assembly.
  • the barrel 2 has a finger plate 2.3 and an inwardly facing wedge sectioned ring 2.4.
  • the nose 2.1 of the barrel and the needle mounting 1.1 may be non-circular as will be described hereinafter with reference to Figure 5 , in order to prevent relative axial rotation.
  • the plunger 3 has an inwardly facing triangular sectioned ring 3.1, an inward facing wedge shaped ring 3.2 and outwardly facing wedge sectioned rings 3.3 and 3.4.
  • the closure piece 4 has a seal 4.1 which is held in place by a wedge section ring 3.2 of plunger 3.
  • the piston 5 carries the seal 5.1 which co-acts with the inner surface of the plunger 3 and a triangular section ring 5.2.
  • the piston 5 includes a probe 5.3 which carries a resilient slit ring 5.4.
  • the ring 5.4 is positioned so that it snaps past internal lip 1.6 before the injection stroke is completed.
  • the closure piece 4 and the piston 5 are temporarily held in contact by the use of an appropriate lubricant between the two mating surfaces 4.2 and 5.5. These are inserted as one piece at the right-hand end of the plunger 3 shown in Figure 1 .
  • the piston 5 is then drawn through the interior of the plunger 3 until the triangular sectioned ring 5.2 snaps past the inward facing triangular ring 3.1, creating a vacuum inside the plunger 3 and holding the piston 5 and the plunger 3 together as one piece.
  • the vacuum is maintained by seals 4.1 and 5.1.
  • the closure piece 4 is thus held at the end of the plunger 3.
  • the capsule assembly it is pre-charged with injectant fluid between the dished needle end 1.9 and the resilient plunger disc 1.8. Also, the assembly is fitted with the needle sheath 1.4 over the needle 1.2, which is held in place by the frangible sealant 1.3.
  • the capsule assembly 1 is passed through the interior of the barrel 2 until the needle mounting 1.1 rests in the nose 2.1 of the barrel.
  • the aperture 2.1 is sufficiently large to allow the passage of the needle 1.2 and the protective, sealed sheath 1.4 through the aperture.
  • the sheath 1.4 affords protection to the needle 1.2 and guidance in entering and locating the capsule assembly in the nose 2.1 of the barrel.
  • the larger size of the nose aperture 2.1 in relation to the diameter of the needle 1.2 enables a bent needle to be retracted as will be evident hereinafter.
  • the or each arm 2.2 abuts against the external lip 1.7 thereby restraining the capsule assembly 1 from inward movement.
  • the seal afforded by the sheath 1.4 prevents inward movement of the plunger 3 being made before the sheath 1.4 has been removed from the needle 1.2.
  • the plunger 3 and the piston 5 are inserted into the barrel 2 as one piece until wedge sectioned ring 3.3 snaps past wedge sectioned ring 2.4. It is not possible thereafter for the plunger to be withdrawn from the barrel.
  • the syringe is thus assembled ready for use.
  • the sheath 1.4 is removed from the needle 1.2.
  • the non-circular construction of the needle mounting 1.1 and the nose 2.1 allows the sheath 1.4 to be rotated independently of its associated components, thereby breaking the seal between them and facilitating removal of the sheath 1.4.
  • the syringe can then be operated according to established practice for disposable syringes.
  • the syringe is gripped by the user such that the plunger 3 is slidably inserted into the barrel 2, with the user gripping the finger plate 2.3.
  • automatic needle retraction is triggered by further pressure on the plunger 3, as will now be described in detail.
  • lip 3.4 snaps past wedge section ring 2.4 thus locking the plunger 3 with the barrel 2 and preventing the plunger from being withdrawn therefrom.
  • Figure 2 illustrates the resulting configuration of the syringe component shown in Figure 1 , after needle retraction has occurred. It will be seen that the needle 1.2 has been withdrawn completely within the barrel 2 thereby obviating the risk of needle stick injury.
  • Figure 3 illustrates an alternative construction in which the energy used to effect retraction is provided by compression spring 6 rather than the vacuum between the plunger 3 and piston 5, of the embodiment of Figure 1 .
  • the spring 6 is located within the plunger 3 and is of the maximum diameter allowed by the internal dimensions of the plunger 3.
  • the triangular section ring 3.1 provides a stop which locates the spring 6.
  • the probe 5.3 is passed through the interior of the spring 6 and inward pressure is applied to face 5.5, moving the piston 5 through the plunger 3 simultaneously compressing the spring 6 until the triangular sectioned ring 5.2 snaps past the triangular sectioned ring 3.1.
  • the spring 6 is now held in compression and the plunger 3 and piston 5 are held together as one piece.
  • closure piece 4 is now fitted into the barrel and held by the wedge sectioned ring 3.2. Operation of the device is as previously described with reference to Figure 1 , with the retraction of the needle being performed under the force of compression spring 6 rather than the vacuum as previously described.
  • Figure 4 illustrates a configuration in which the compression spring 6 is located within the barrel 2, so as to surround the capsule assembly 1.
  • the capsule assembly 1 is passed through the interior of the spring 6 which is compressed against the locally increased diameter 1.5 as the capsule assembly 1 is loaded into place.
  • the capsule assembly 1 is held in position and the spring 6 is held in compression by the or each arm 2.2. acting on the external lip 1.7.
  • the piston 5 has a triangularly shaped groove 5.2.
  • assembly is achieved as previously described, except that the piston 5 and the plunger 3 are joined by pushing the piston 5 into the plunger 3 until the triangularly shaped groove 5.2 is retained by the triangular section ring 3.1.
  • Operation of the embodiment of Figure 4 is carried out as previously described except that when the final inward pressure on the plunger 3 snaps the triangular section ring 3.1 out of the groove 5.2, the spring 6 forces the capsule assembly 1 and the piston 5 into the plunger 3.
  • Figure 5A illustrates in perspective the capsule assembly 1 including the needle 1.2 and needle sheath 1.4 with its rectangular i.e. non-cylindrical nose portion 1.1 which co-acts with the close fitting, similarly shaped aperture in the barrel 2 (not shown in Figure 5 ).
  • the needle and capsule assembly 1 is prevented by the co-acting non-circular faces of the assembly 1 and barrel aperture 2.1 when the needle sheath is twisted so as to break the seal 1.3 and facilitate removal of the sheath.
  • other means of achieving this may be used such as an off-set pin and socket or other means of producing non-rotary engagement between the capsule assembly 1 and the barrel 2.
  • Figure 5B illustrates an alternative configuration in which the capsule assembly 1 can be retained in the housing 2 before retraction of the needle is initiated, using a clip 7.
  • the described embodiments of the invention thus provide for safe and reliable operation of a pre-loaded syringe and have the advantage that the capsule assembly 1 containing the injectant 1.10 is pre-loaded and sealed under controlled conditions ready for incorporation into the syringe.
  • the injectant and the quantity thereof may be identified on the capsule, for example by means of a barcode which may be magnetic and may provide data for inclusion into the patients record, stock control and quality control purposes.
  • the user is not required to expel excess air from the needle prior to use and no calibrations for the dose are necessary because the dose is pre-set by the volume of injectant included into the capsule assembly 1. It will be understood that partial rotation of the needle sheath 1.4 breaks the seal and facilitates removal of the needle sheath from the needle 1.4 immediately prior to use. Seepage and spillage of the injectant are prevented as previously described.
  • the syringe according to the invention is reliable, instinctive in its operation and capable of being used with one hand. Furthermore, the needle is automatically retracted completely following the injection and, because the aperture 2.1 in the nose of barrel is relatively large, it has the capacity to retract a bent needle. Furthermore, re-exposure of the needle cannot occur after the injection thereby minimising the risk of a needle stick injury. Also, accidental retraction of the needle before the injection is prevented.
  • the described examples of syringe according to the invention are so configured that there are locked closed after use to provide for compact and safe disposal.
  • the described syringes can be manufactured at low cost.

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Environmental & Geological Engineering (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)

Claims (23)

  1. Seringue incluant une aiguille (1.2) rétractable par l'énergie stockée lors de l'achèvement d'une course d'injection, comprenant un boîtier (2) et un plongeur (3), caractérisée en ce qu'un ensemble de capsule scellé (1) contenant l'injectant est installé dans le boîtier (2), et l'ensemble de capsule scellé (1) comprend un ensemble d'aiguille comprenant un montage d'aiguille (1.1), une aiguille (1.2), un scellement pouvant être rompu (1.3) et une gaine de protection d'aiguille (1.4) couvrant l'aiguille (1.2), où la gaine de protection d'aiguille scellée (1.4) empêche un mouvement du plongeur (3) dans le boîtier (2) avant la rupture du scellement (1.3) et du retrait de la gaine de protection (1.4).
  2. Seringue selon la revendication 1, dans laquelle seulement l'aiguille et l'ensemble de capsule (1) viennent en contact avec l'injectant.
  3. Seringue selon la revendication 1 ou la revendication 2, dans laquelle la gaine de protection d'aiguille (1.4) est munie d'un codage indiquant les constituants de l'injectant ainsi que la quantité.
  4. Seringue selon la revendication 3, dans laquelle le codage est un code à barres.
  5. Seringue selon la revendication 3, dans laquelle le codage est magnétique.
  6. Seringue selon la revendication 3, dans laquelle le codage fournit des données pour les dossiers des patient, pour la gestion des stocks et pour le contrôle de qualité.
  7. Seringue selon l'une quelconque des revendications précédentes, dans laquelle l'énergie stockée est réalisée par un vide.
  8. Seringue selon les revendications 1 à 6, dans laquelle l'énergie stockée est retenue dans un ressort (6).
  9. Seringue selon la revendication 8, dans laquelle le ressort (6) est maintenu en compression et est situé dans le plongeur (3).
  10. Seringue selon la revendication 8, dans laquelle le ressort (6) est maintenu en compression et est situé autour de l'ensemble de capsule (1).
  11. Seringue selon les revendications 7 et 9, dans laquelle la partie rétractable du plongeur (3) est couplée à la capsule (1) et à l'ensemble d'aiguille proche de l'achèvement de la course d'injection.
  12. Seringue selon l'une quelconque des revendications précédentes, dans laquelle le plongeur (3) est apte à s'affaisser axialement à une surcharge réglée.
  13. Seringue selon l'une quelconque des revendications précédentes, dans laquelle l'ensemble d'aiguille et de capsule (1) est retenu avant la rétraction par un cliquet (2.2) déplaçable par le plongeur (3) lors de l'achèvement de la course d'injection.
  14. Seringue selon la revendication 13, dans laquelle ledit cliquet (2.2) est une propriété réalisée intégralement du boîtier (2).
  15. Seringue selon la revendication 13, dans laquelle ledit cliquet est un composant ou ensemble séparé.
  16. Seringue selon l'une quelconque des revendications précédentes, dans laquelle l'ensemble d'aiguille et de capsule (1) peut être installé à travers le boîtier (2) de la seringue.
  17. Seringue selon l'une quelconque des revendications précédentes, dans laquelle l'extrémité d'aiguille du boîtier (2) est munie d'une ouverture non cylindrique à travers laquelle l'aiguille (1.2) et la gaine de protection (1.4) peuvent passer dans laquelle une section non cylindrique de coaction de l'ensemble de capsule (1) entre pour permettre l'application d'un couple à la gaine de protection (1.4) pour rompre le scellement (1.3) et pour faciliter son retrait.
  18. Seringue selon la revendication 17, dans laquelle le jeu réalisé par l'ouverture non cylindrique dans le boîtier (2) permet à l'énergie stockée de rétracter et retenir dans le boîtier (2) une aiguille courbée (1.2).
  19. Seringue selon les revendications 1 à 16, dans laquelle l'extrémité d'aiguille du boîtier (2) est munie d'une ouverture cylindrique à travers laquelle l'aiguille (1.2) et la gaine de protection (1.4) peuvent passer et dans laquelle une section cylindrique de coaction de l'ensemble de capsule (1) entre, un mouvement de rotation relatif étant empêché par une saillie et un logement récepteur en coaction sur les deux parties, pour permettre l'application d'un couple à la gaine de protection (1.4) pour rompre le scellement (1.3) et pour faciliter son retrait.
  20. Seringue selon la revendication 19, dans laquelle le jeu réalisé par l'ouverture cylindrique dans le boîtier (2) permet à l'énergie stockée de rétracter et retenir dans le boîtier (2) une aiguille courbée (1.2).
  21. Seringue selon l'une quelconque des revendications précédentes, dans laquelle l'ensemble à aiguille et à capsule (1) contient un disque résilient déplaçable axialement (1.8) qui, sous pression exercée vers l'intérieur, expulsera l'injectant.
  22. Seringue selon la revendication 21, dans laquelle la résilience du disque (1.8) permet la distorsion de sa forme naturelle sous pression de la course d'injection de répliquer la géométrie de l'aiguille et de la capsule (1) pour obtenir une évacuation complète de la capsule (1).
  23. Seringue selon la revendication 21, dans laquelle la résilience du disque (1.8) permet le retour à sa forme naturelle après le relâchement de la pression de la course d'injection et de ce fait l'aspiration de tout injectant résiduel du perçage d'aiguille.
EP01911998.1A 2000-03-24 2001-03-20 Seringue hypodermique Expired - Lifetime EP1272240B8 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0007269.4A GB0007269D0 (en) 2000-03-24 2000-03-24 Improvements in or relating to hypodermic syringes
GB0007269 2000-03-24
PCT/GB2001/001228 WO2001072362A1 (fr) 2000-03-24 2001-03-20 Seringue hypodermique

Publications (3)

Publication Number Publication Date
EP1272240A1 EP1272240A1 (fr) 2003-01-08
EP1272240B1 true EP1272240B1 (fr) 2014-04-30
EP1272240B8 EP1272240B8 (fr) 2014-06-04

Family

ID=9888416

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01911998.1A Expired - Lifetime EP1272240B8 (fr) 2000-03-24 2001-03-20 Seringue hypodermique

Country Status (6)

Country Link
US (1) US20030163092A1 (fr)
EP (1) EP1272240B8 (fr)
JP (1) JP2003527936A (fr)
AU (1) AU2001240916A1 (fr)
GB (1) GB0007269D0 (fr)
WO (1) WO2001072362A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0222731D0 (en) * 2002-10-01 2002-11-06 Parker David W Improvements in or relating to hypodermic syringes
AU2003903990A0 (en) * 2003-07-31 2003-08-14 Medigard Pty Ltd Cannula/catheter introducer
GB0420640D0 (en) * 2004-09-16 2004-10-20 Speriam Securities Inc A syringe
US7699814B2 (en) * 2005-05-17 2010-04-20 Ralph Lande Syringe sheath
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Also Published As

Publication number Publication date
EP1272240B8 (fr) 2014-06-04
JP2003527936A (ja) 2003-09-24
GB0007269D0 (en) 2000-05-17
AU2001240916A1 (en) 2001-10-08
EP1272240A1 (fr) 2003-01-08
WO2001072362A1 (fr) 2001-10-04
US20030163092A1 (en) 2003-08-28

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